A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7265



Internal ID15536599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:68180355..68213762hg38UCSC Ensembl
Outerchr16:68214258..68247665hg19UCSC Ensembl
Outerchr16:66771759..66805166hg18UCSC Ensembl
Outerchr16:66771759..66805166hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg386030
hg196030
hg186030
hg176030
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1846
Supporting Variants
SamplesNA12156
Known GenesNFATC3
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv7265
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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